The hunter syndrome market size is expected to witness 6.9 % CAGR over the forecast period of 2019 to 2026. Rise in incidences of mucopolysaccharidoses II in male population across the globe contributes to the market growth. In addition, growing R&D activities pertaining to gene editing is also instrumental in shaping the market growth throughout the forecast period.
Hunter syndrome is a genetically inherited disease and caused due to a particular defect in the gene formation. The defect results in lack of production of major enzymes that enables a breakdown of sugary molecules in diet, termed as mucopolysaccharides. These get formed in the body of patient and leads into damage of vital organs. As a part of treatment, the patients are dosed with frequent replacements with enzymes that are responsible for synthesis of mucopolysaccharides in order to prevent their accumulation.
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In this condition, the patient suffers from neurodegenerative changes, enlargement of periventricular spaces, and tissue atrophy. At present, there is no such treatment available for hunter syndrome in developing countries and to some extent in developed countries. Government run campaigns and rehab camps are most likely to help in countering the disease.